Allele Registry

Canonical Allele Identifier: PA2827921981

Gene: SCN5A HGNC NCBI

ClinVar Allele:

1296638

ClinVar RCV:

RCV001770875

ClinVar Variation:

1306695

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Val563Leu	CA352146717 NM_001354701.2:c.1687G>T CA352146720 NM_001354701.2:c.1687G>C